549 related articles for article (PubMed ID: 11285240)
1. Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping.
Buratti E; Dörk T; Zuccato E; Pagani F; Romano M; Baralle FE
EMBO J; 2001 Apr; 20(7):1774-84. PubMed ID: 11285240
[TBL] [Abstract][Full Text] [Related]
2. An intronic polypyrimidine-rich element downstream of the donor site modulates cystic fibrosis transmembrane conductance regulator exon 9 alternative splicing.
Zuccato E; Buratti E; Stuani C; Baralle FE; Pagani F
J Biol Chem; 2004 Apr; 279(17):16980-8. PubMed ID: 14966131
[TBL] [Abstract][Full Text] [Related]
3. Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9.
Buratti E; Baralle FE
J Biol Chem; 2001 Sep; 276(39):36337-43. PubMed ID: 11470789
[TBL] [Abstract][Full Text] [Related]
4. Splicing factors induce cystic fibrosis transmembrane regulator exon 9 skipping through a nonevolutionary conserved intronic element.
Pagani F; Buratti E; Stuani C; Romano M; Zuccato E; Niksic M; Giglio L; Faraguna D; Baralle FE
J Biol Chem; 2000 Jul; 275(28):21041-7. PubMed ID: 10766763
[TBL] [Abstract][Full Text] [Related]
5. SR protein-mediated inhibition of CFTR exon 9 inclusion: molecular characterization of the intronic splicing silencer.
Buratti E; Stuani C; De Prato G; Baralle FE
Nucleic Acids Res; 2007; 35(13):4359-68. PubMed ID: 17576688
[TBL] [Abstract][Full Text] [Related]
6. CELF proteins regulate CFTR pre-mRNA splicing: essential role of the divergent domain of ETR-3.
Dujardin G; Buratti E; Charlet-Berguerand N; Martins de Araujo M; Mbopda A; Le Jossic-Corcos C; Pagani F; Ferec C; Corcos L
Nucleic Acids Res; 2010 Nov; 38(20):7273-85. PubMed ID: 20631008
[TBL] [Abstract][Full Text] [Related]
7. Functional analysis of cis-acting elements regulating the alternative splicing of human CFTR exon 9.
Niksic M; Romano M; Buratti E; Pagani F; Baralle FE
Hum Mol Genet; 1999 Dec; 8(13):2339-49. PubMed ID: 10556281
[TBL] [Abstract][Full Text] [Related]
8. Cellular and viral splicing factors can modify the splicing pattern of CFTR transcripts carrying splicing mutations.
Nissim-Rafinia M; Chiba-Falek O; Sharon G; Boss A; Kerem B
Hum Mol Genet; 2000 Jul; 9(12):1771-8. PubMed ID: 10915765
[TBL] [Abstract][Full Text] [Related]
9. A T3 allele in the CFTR gene exacerbates exon 9 skipping in vas deferens and epididymal cell lines and is associated with Congenital Bilateral Absence of Vas Deferens (CBAVD).
Disset A; Michot C; Harris A; Buratti E; Claustres M; Tuffery-Giraud S
Hum Mutat; 2005 Jan; 25(1):72-81. PubMed ID: 15580565
[TBL] [Abstract][Full Text] [Related]
10. Nuclear factor TDP-43 binds to the polymorphic TG repeats in CFTR intron 8 and causes skipping of exon 9: a functional link with disease penetrance.
Buratti E; Brindisi A; Pagani F; Baralle FE
Am J Hum Genet; 2004 Jun; 74(6):1322-5. PubMed ID: 15195661
[No Abstract] [Full Text] [Related]
11. Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene.
Mercado PA; Ayala YM; Romano M; Buratti E; Baralle FE
Nucleic Acids Res; 2005; 33(18):6000-10. PubMed ID: 16254078
[TBL] [Abstract][Full Text] [Related]
12. Combined computational-experimental analyses of CFTR exon strength uncover predictability of exon-skipping level.
Aissat A; de Becdelièvre A; Golmard L; Vasseur C; Costa C; Chaoui A; Martin N; Costes B; Goossens M; Girodon E; Fanen P; Hinzpeter A
Hum Mutat; 2013 Jun; 34(6):873-81. PubMed ID: 23420618
[TBL] [Abstract][Full Text] [Related]
13. Characterization of disease-associated mutations affecting an exonic splicing enhancer and two cryptic splice sites in exon 13 of the cystic fibrosis transmembrane conductance regulator gene.
Aznarez I; Chan EM; Zielenski J; Blencowe BJ; Tsui LC
Hum Mol Genet; 2003 Aug; 12(16):2031-40. PubMed ID: 12913074
[TBL] [Abstract][Full Text] [Related]
14. An exonic splicing enhancer offsets the atypical GU-rich 3' splice site of human apolipoprotein A-II exon 3.
Arrisi-Mercado P; Romano M; Muro AF; Baralle FE
J Biol Chem; 2004 Sep; 279(38):39331-9. PubMed ID: 15247216
[TBL] [Abstract][Full Text] [Related]
15. Characterization of a disease-associated mutation affecting a putative splicing regulatory element in intron 6b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
Faà V; Incani F; Meloni A; Corda D; Masala M; Baffico AM; Seia M; Cao A; Rosatelli MC
J Biol Chem; 2009 Oct; 284(44):30024-31. PubMed ID: 19759008
[TBL] [Abstract][Full Text] [Related]
16. Binding sites for Rev and ASF/SF2 map to a 55-nucleotide purine-rich exonic element in equine infectious anemia virus RNA.
Chung H ; Derse D
J Biol Chem; 2001 Jun; 276(22):18960-7. PubMed ID: 11278454
[TBL] [Abstract][Full Text] [Related]
17. The role of common single-nucleotide polymorphisms on exon 9 and exon 12 skipping in nonmutated CFTR alleles.
Steiner B; Truninger K; Sanz J; Schaller A; Gallati S
Hum Mutat; 2004 Aug; 24(2):120-9. PubMed ID: 15241793
[TBL] [Abstract][Full Text] [Related]
18. Interactions among SR proteins, an exonic splicing enhancer, and a lentivirus Rev protein regulate alternative splicing.
Gontarek RR; Derse D
Mol Cell Biol; 1996 May; 16(5):2325-31. PubMed ID: 8628299
[TBL] [Abstract][Full Text] [Related]
19. Antagonistic factors control the unproductive splicing of SC35 terminal intron.
Dreumont N; Hardy S; Behm-Ansmant I; Kister L; Branlant C; Stévenin J; Bourgeois CF
Nucleic Acids Res; 2010 Mar; 38(4):1353-66. PubMed ID: 19965769
[TBL] [Abstract][Full Text] [Related]
20. TDP43 depletion rescues aberrant CFTR exon 9 skipping.
Ayala YM; Pagani F; Baralle FE
FEBS Lett; 2006 Feb; 580(5):1339-44. PubMed ID: 16458894
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]